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Have
you been harmed by this device and are seeking legal advice? Are you
looking for more information about the recall? Guidant
Corporation made the Ancure
Aorta Patch which is used to fix bulging walls of the main artery
that carries blood away from the heart. These bulges are
called abdominal aortic aneurysms or AAA.
Learn
about the Guidant defibrillator recall by clicking
on the links at the right column or the links below to find your
attorney in your city or state and to read more information such as
the types of Guidant models that have been recalled and the growing
regulatory issues: "The New York Times and Wall
Street Journal reported Guidant Corp. continued to sell potentially
flawed implantable heart defibrillators for months after making
changes to the device to fix an electrical problem. Reports
indicate Guidant could face legal and regulatory problems for
selling older devices with a possible flaw while improved ones were
available." http://www.onlinelawyersource.com/news/Guidant-heart-defibrillat.html.
California
attorneys: http://www.alllaw.com/state_resources/California/
Southern
California lawyers: http://www.southerncalifornialawyers.com/
Lawyers by city: http://www.lawyers-by-city.com/
Guidant recalled models and news
articles: http://www.onlinelawyersource.com/guidant/recalled-defibrillators.html
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